New self-assembled one-dimensional nickel coordination polymers and hydrogen-bonded networks

2003 ◽  
pp. 631-637 ◽  
Author(s):  
Dejana Vujovic ◽  
Helgard G. Raubenheimer ◽  
Luigi R. Nassimbeni
Keyword(s):  
Coordination Polymers ◽  
One Dimensional ◽  
Self Assembled ◽  
Hydrogen Bonded

One-dimensional Hydrogen-bonded Chloride-Hydrate Assembly {[(H2O)4Cl2]2–}∞

2007 ◽  
Vol 62 (4) ◽  
pp. 491-494 ◽  
Author(s):  
Ji-Xiang Dai ◽  
Fang-Hui Wu ◽  
Wen-Rui Yao ◽  
Qian-Feng Zhang
Keyword(s):  
Hydrogen Bonding ◽  
Bond Length ◽  
Chloride Ions ◽  
Water Molecules ◽  
One Dimensional ◽  
Self Assembled ◽  
Chloride Hydrate ◽  
Hydrogen Bonded

A hydrogen-bonded chloride-hydrate assembly {[(H2O)4Cl2]2−}∞ has been ion-countered by the complex cations [Fe([9]aneS3)2]2+ ([9]aneS3 = 1,4,7-trithiacyclononane). In {[(H2O)4Cl2]2−}∞, four water molecules and two chloride ions are self-assembled to form a one-dimensional supramolecular array of O-H···O and O-H···Cl hydrogen bonding, which consists of fused fourand six-membered rings. The discrete cation [Fe([9]aneS3)2]2+ has a nearly regular octahedral FeS6 core with an average Fe-S bond length of 2.2586(5) Å .

One-dimensional single-helix coordination polymer self-assembled by a crown-ether appended-N-heteroacene radical anion

2019 ◽  
Vol 48 (35) ◽  
pp. 13125-13129 ◽  
Author(s):  
Kyosuke Isoda ◽  
Hinako Takahashi ◽  
Yuichiro Mutoh ◽  
Norihisa Hoshino ◽  
Tomoyuki Akutagawa
Keyword(s):  
Coordination Polymer ◽  
Crown Ether ◽  
Coordination Polymers ◽  
Radical Anion ◽  
Radical Anions ◽  
One Dimensional ◽  
Self Assembled ◽  
Single Helix

Radical anions based on crown-ether appended N-heteroacene with Na+ self-assemble one-dimensional helical coordination polymers.

Anion and solvent controlled growth of crystalline and amorphous zinc(II) coordination polymers and a molecular complex

2021 ◽  
Author(s):  
Claire Deville ◽  
Henrik Særkjær Jeppesen ◽  
Vickie McKee ◽  
Nina Lock
Keyword(s):  
Coordination Polymers ◽  
Molecular Complex ◽  
Research Field ◽  
Metal Coordination ◽  
Controlled Growth ◽  
Bottom Up ◽  
One Dimensional

Controlled bottom-up synthesis of amorphous coordination polymers with tailored metal coordination is a research field in its infancy. In this study, synthesis control was achieved to selectively prepare one-dimensional (1D)...

On-Surface Synthesis of One-Dimensional Coordination Polymers with Tailored Magnetic Anisotropy

2021 ◽  
Author(s):  
Benjamin Mallada ◽  
Piotr Błoński ◽  
Rostislav Langer ◽  
Pavel Jelínek ◽  
Michal Otyepka ◽  
...  
Keyword(s):  
Magnetic Anisotropy ◽  
Coordination Polymers ◽  
One Dimensional

1D Mn(III) Coordination Polymers Exhibiting Chiral Symmetry Breaking and Weak Ferromagnetism

2021 ◽  
Author(s):  
Aoi Hara ◽  
Sotaro Kusumoto ◽  
Yoshihiro Sekine ◽  
Jack Harrowfield ◽  
Yang Kim ◽  
...  
Keyword(s):  
Symmetry Breaking ◽  
Chiral Symmetry ◽  
Coordination Polymers ◽  
Chiral Symmetry Breaking ◽  
Weak Ferromagnetism ◽  
Chiral Ligands ◽  
One Dimensional

Mn(III) complexes with the non-chiral ligands, (E)-N-(2-((2-aminobenzylidene)amino)-2-methylpropyl)-5-X-2-hydroxybenzamide (HLX, X = H, Cl, Br, and I), crystallise as chiral conglomerates containing amide oxygen-bridged one-dimensional coordination polymers that exhibit weak ferromagnetism. The...

Concomitant polymorphs of 1,3-bis(3-fluorophenyl)urea

2016 ◽  
Vol 72 (9) ◽  
pp. 692-696 ◽  
Author(s):  
Christina A. Capacci-Daniel ◽  
Jeffery A. Bertke ◽  
Shoaleh Dehghan ◽  
Rupa Hiremath-Darji ◽  
Jennifer A. Swift
Keyword(s):  
Hydrogen Bonding ◽  
Crystal Engineering ◽  
Structural Motif ◽  
Parallel Orientation ◽  
One Dimensional ◽  
Monoclinic Form ◽  
Engineering Studies ◽  
Hydrogen Bonded

Hydrogen bonding between urea functionalities is a common structural motif employed in crystal-engineering studies. Crystallization of 1,3-bis(3-fluorophenyl)urea, C13H10F2N2O, from many solvents yielded concomitant mixtures of at least two polymorphs. In the monoclinic form, one-dimensional chains of hydrogen-bonded urea molecules align in an antiparallel orientation, as is typical of many diphenylureas. In the orthorhombic form, one-dimensional chains of hydrogen-bonded urea molecules have a parallel orientation rarely observed in symmetrically substituted diphenylureas.

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